Meyer R, Candrian U, Lüthy J
University of Berne, Department of Food Chemistry, Switzerland.
J AOAC Int. 1994 May-Jun;77(3):617-22.
A new method for the specific, sensitive, and semiquantitative detection of pork (Sus scrofa) in heat-treated meat products has been developed. DNA was isolated from meat samples by using a DNA-binding resin and subjected to polymerase chain reaction (PCR) analysis. First, oligonucleotides yielding a specific 137-base-pair (bp) fragment from eucaryotic DNA amplified from a highly conserved region of the 18-S ribosomal gene was used to assess DNA quality. Second, the presence of pork DNA was determined with specific oligonucleotides yielding a 108-bp fragment amplified from the porcine growth hormone gene. The test detected pork in fresh or heated meat mixtures of pork in beef at levels below 2%. This approach was superior to commercially available immunological tests that were not able to detect levels of pork less than 20% in cooked meat or less than 10% in fresh meat.
已开发出一种用于特异性、灵敏且半定量检测热处理肉制品中猪肉(猪)的新方法。使用DNA结合树脂从肉样中分离DNA,并进行聚合酶链反应(PCR)分析。首先,从18 - S核糖体基因的高度保守区域扩增的真核DNA中产生特定137碱基对(bp)片段的寡核苷酸用于评估DNA质量。其次,用从猪生长激素基因扩增出108 - bp片段的特异性寡核苷酸确定猪肉DNA的存在。该测试可检测出牛肉中新鲜或加热的猪肉混合肉中含量低于2%的猪肉。这种方法优于市售的免疫检测方法,后者无法检测出熟肉中低于20%或鲜肉中低于10%的猪肉含量。